Last updated: 11/07/2018 16:04:36
Chlorproguanil-Dapsone-Artesunate (CDA) Versus Chlorproguanil-Dapsone (LAPDAP) For Uncomplicated Malaria
Clinicaltrials.gov ID
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: A multi-centre, randomised, double-blind study to compare the efficacy and safety of chlorproguanil-dapsone-artesunate versus chlorproguanil-dapsone in the treatment of acute uncomplicated Plasmodium falciparum malaria in children, adolescents and adults in Africa.
Trial description: CDA is a combination of chlorproguanil, dapsone and artesunate, being developed in a public-private partnership with the Medicines for Malaria Venture (MMV), World Health Organisation (WHO-TDR) and academic partners from the London School of Hygiene and Tropical Medicine, University of Liverpool and the Liverpool School of Tropical Medicine as a treatment for acute uncomplicated P. falciparum malaria.The combination of chlorproguanil HCl (CPG) and dapsone (DDS) as chlorproguanil-dapsone has already been shown to be efficacious against P.falciparum in adults and children in Sub-Sahara Africa. The addition of artesunate to LAPDAP has been demonstrated to increase the parasite kill rate as demonstrated in the phase II study, and reduce the chance of any parasites escaping treatment over the 3-day course. The addition of artesunate is also anticipated to have the population benefit of protection against the development of resistant strains of P.falciparum, although it will not be possible to demonstrate this in a clinical trial. One further population benefit of the artemisinin drugs are their ability to suppress the sexual forms of the parasite (gametocytes), which should reduce infectivity after antimalarial treatment and potentially lower transmission rates with widespread use, including the spread of any parasites resistant to the partner drug.The aims of this phase III study are to compare the efficacy of a fixed ratio combination tablet of CDA to chlorproguanil-dapsone, and collect supporting safety data. This will be a multi-centre, double-blind, double-dummy, randomised trial, in children, adolescents and adults, with chlorproguanil-dapsone as a comparator.
Primary purpose:
Treatment
Trial design:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Allocation:
Randomized
Primary outcomes:
Parasitological cure rate, PCR-corrected, at day 28, in the per-protocol population. Parasitological cure rate is defined as the clearance of the initial malaria infection by day 7 and remaining free of this infection to the day of assessment.
Timeframe: N/A
Secondary outcomes:
The proportion of subjects with parasites remaining at 24 hours post-first dose by treatment group. Parasitological cure rate, PCR-corrected, at day 14, by treatment group.
Timeframe: N/A
Interventions:
Enrollment:
900
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Lucio Luzzatto, Naomi Richardson, Nick Carter, Stephan Duparc, Zul Premji, Alfred Tiono, Allan Pamba. Clinical spectrum of hemolytic anemia in glucose-6-phosphate dehydrogenase-deficient children receiving dapsone. Blood. 2012;120:4123-4133.
Medical condition
Malaria, Falciparum
Product
artesunate, artesunate/chlorproguanil/dapsone, chlorproguanil, dapsone
Collaborators
Not applicable
Study date(s)
April 2006 to May 2007
Type
Interventional
Phase
3
Participation criteria
Sex
Female & Male
Age
12+ years
Accepts healthy volunteers
No
- Inclusion criteria:
- Acute, uncomplicated P.falciparum malaria, microscopically confirmed infection.
Inclusion and exclusion criteria
Inclusion criteria:
- Inclusion criteria:
- Acute, uncomplicated P.falciparum malaria, microscopically confirmed infection.
- Temperature at screening of 37.5oC or over or confirmed history of fever within previous 24-hours.
- Weight 7.5kg or over , no upper weight limit.
- Screening haemoglobin (Hb) of 7g/dl, or more or haematocrit of 25% or over(if Hb not available at screening).
- Willingness to comply with the study visits and procedures, as outlined in the informed consent form.
- Written or oral witnessed consent obtained from subject, parent or guardian.
- Assent is given by a child aged 12 to <18years, in addition to the consent of their parent or guardian. Exclusion criteria:
- Features of severe/complicated falciparum malaria.
- Hypersensitivity to active substances (chlorproguanil, dapsone, artesunate), or excipients of the investigational products.
- Known allergy to biguanides, sulphones, sulphonamides or artemisinin derived products.
- Known history of G6PD deficiency.
- Infants with a history of hyperbilirubinaemia during the neonatal period.
- Evidence of any concomitant infection at the time of presentation (including P. vivax, P. ovale and P. malariae).
- Use of concomitant medications that may induce haemolysis or haemolytic anaemia from the WHO (World Health Organization) list of essential drugs.
- Any other underlying disease that may compromise the diagnosis and the evaluation of the response to the study medication (including clinical symptoms of immunosuppression, tuberculosis, bacterial infection; cardiac or pulmonary disease).
- Malnutrition, defined as a child whose weight-for-height is below -3 standard deviations or less than 70% of the median of the NCHS/WHO normalised reference values
- Treatment within the past three months with mefloquine or mefloquine-sulphadoxine-pyrimethamine; twenty-eight days with sulphadoxine/pyrimethamine, sulfalene/pyrimethamine, lumefantrine or artemether/lumefantrine, amodiaquine, atovaquone or atovaquone/proguanil, halofantrine; 14-days with chlorproguanil/dapsone, or 7-days with quinine (full course), proguanil, artemisinin, tetracycline doxycycline or clindamycin.
- Positive sulphadoxine/pyrimethamine urine screen for ‘unknown’ antimalarial drug use in prior 28-days.
- Use of an investigational drug within 30 days or 5 half-lives whichever is the longer.
- Previous participation in this study.
- Female subjects of child-bearing potential who have had a positive pregnancy test at enrolment, or do not give their consent to take a pregnancy test.
- Female subjects who will be breast-feeding an infant for the duration of the study.
Trial location(s)
Showing 1 - 6 of 7 Results
Study documents
Clinical study report
Available language(s): English
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Refer to study documents
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
2007-23-05
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
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